Literature DB >> 22133538

Neonatal screening for lysosomal storage disorders.

Janice Fletcher1, Bridget Wilcken.   

Abstract

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Year:  2011        PMID： 22133538     DOI： 10.1016/S0140-6736(11)61744-3

Source DB:  PubMed          Journal:  Lancet        ISSN： 0140-6736            Impact factor:   79.321


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  4 in total

1.  Determination of Biological Variance and Validation of a Fluorometric Assay for Measurement of α-l-Iduronidase Activity in Dried Blood Spots Samples: The First Experience in Iran.

Authors:  Mohammad Abdi; Mohammad Said Hakhamaneshi; Mohammad Reza Alaei; Namam-Ali Azadi; Rahim Vakili; Daniel Zamanfar; Mohammad Taghikhani; Shohreh Khatami
Journal:  Indian J Clin Biochem       Date:  2014-07-30

Review 2.  Lysosomal diseases: diagnostic update.

Authors:  Bryan Winchester
Journal:  J Inherit Metab Dis       Date:  2014-04-08       Impact factor: 4.982

Review 3.  The evolution of blood-spot newborn screening.

Authors:  Kaustuv Bhattacharya; Tiffany Wotton; Veronica Wiley
Journal:  Transl Pediatr       Date:  2014-04

Review 4.  Mucopolysaccharidosis type III (Sanfilippo syndrome) and misdiagnosis of idiopathic developmental delay, attention deficit/hyperactivity disorder or autism spectrum disorder.

Authors:  Frits A Wijburg; Grzegorz Węgrzyn; Barbara K Burton; Anna Tylki-Szymańska
Journal:  Acta Paediatr       Date:  2013-02-06       Impact factor: 2.299
  4 in total

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